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Volumn , Issue , 2011, Pages 36-63

Multivalent glycocalixarenes

Author keywords

Calixarenes; Cell transfection; Lectin inhibition; Multivalent effect; Tumor targeting

Indexed keywords


EID: 84882852769     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.2174/978160805277611101010036     Document Type: Chapter
Times cited : (14)

References (72)
  • 1
    • 0027318961 scopus 로고
    • Biological roles of oligosaccharides: all the theories are correct
    • Varki, A. Biological roles of oligosaccharides: all the theories are correct. Glycobiology, 1993, 3, 97-130.
    • (1993) Glycobiology , vol.3 , pp. 97-130
    • Varki, A.1
  • 2
    • 11544358874 scopus 로고    scopus 로고
    • Lectins: Carbohydrate-specific proteins that mediate cellular recognition
    • Lis, H.; Sharon, N. Lectins: Carbohydrate-specific proteins that mediate cellular recognition. Chem. Rev., 1998, 98, 637-674.
    • (1998) Chem. Rev. , vol.98 , pp. 637-674
    • Lis, H.1    Sharon, N.2
  • 3
    • 84882929173 scopus 로고    scopus 로고
    • Ed. The sugar code: Fundamentals of glycosciences; Wiley-Blackwell: Weinheim
    • Gabius H.-J. Ed. The sugar code: Fundamentals of glycosciences; Wiley-Blackwell: Weinheim, 2009.
    • (2009)
    • Gabius, H.-J.1
  • 4
    • 0000358206 scopus 로고
    • Carbohydrate-protein interactions - Basis of glycobiology
    • Lee, Y.C.; Lee, R.T. Carbohydrate-protein interactions - Basis of glycobiology. Acc. Chem. Res., 1995, 28, 321-327.
    • (1995) Acc. Chem. Res. , vol.28 , pp. 321-327
    • Lee, Y.C.1    Lee, R.T.2
  • 5
    • 0032476812 scopus 로고    scopus 로고
    • Polyvalent interactions in biological systems: Implications for design and use of multivalent ligands and inhibitors
    • Mammen, M.; Choi, S.-K.; Whitesides, G.M. Polyvalent interactions in biological systems: Implications for design and use of multivalent ligands and inhibitors. Angew. Chem. Int. Ed., 1998, 37, 2755-2794.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2755-2794
    • Mammen, M.1    Choi, S.-K.2    Whitesides, G.M.3
  • 7
    • 78649377989 scopus 로고    scopus 로고
    • Calixarenes: from biomimetic receptors to multivalent ligands for biomolecular recognition
    • Sansone, F.; Baldini, L.; Casnati, A.; Ungaro, R. Calixarenes: from biomimetic receptors to multivalent ligands for biomolecular recognition. New J. Chem., 2010, 34, 2715-2728.
    • (2010) New J. Chem. , vol.34 , pp. 2715-2728
    • Sansone, F.1    Baldini, L.2    Casnati, A.3    Ungaro, R.4
  • 8
    • 77954914845 scopus 로고    scopus 로고
    • Design and creativity in synthesis of multivalent neoglycoconjugates
    • In: Advances in Carbohydrate Chemistry and Biochemistry; Derek, H., Ed.; Academic Press
    • Chabre, Y.M.; Roy, R. Design and creativity in synthesis of multivalent neoglycoconjugates. In: Advances in Carbohydrate Chemistry and Biochemistry; Derek, H., Ed.; Academic Press: 2010; Vol. 63, pp. 165-393.
    • (2010) , vol.63 , pp. 165-393
    • Chabre, Y.M.1    Roy, R.2
  • 9
    • 10644280152 scopus 로고    scopus 로고
    • Multivalency in supramolecular chemistry and nanofabrication
    • Mulder, A.; Huskens, J.; Reinhoudt, D.N. Multivalency in supramolecular chemistry and nanofabrication. Org. Biomol. Chem., 2004, 2, 3409-3424.
    • (2004) Org. Biomol. Chem. , vol.2 , pp. 3409-3424
    • Mulder, A.1    Huskens, J.2    Reinhoudt, D.N.3
  • 10
    • 23944462030 scopus 로고    scopus 로고
    • Synthetic Multivalent Molecules
    • John Wiley & Sons, Inc.: Hoboken, New Jersey
    • Choi, S.-K. Synthetic Multivalent Molecules, John Wiley & Sons, Inc.: Hoboken, New Jersey, 2004.
    • (2004)
    • Choi, S.-K.1
  • 11
    • 0019407381 scopus 로고
    • On the attribution and additivity of binding energies
    • Jenks, W.P. On the attribution and additivity of binding energies. Proc. Natl. Acad. Sci. USA, 1981, 78, 4046-4050.
    • (1981) Proc. Natl. Acad. Sci. USA , vol.78 , pp. 4046-4050
    • Jenks, W.P.1
  • 12
    • 0347694971 scopus 로고    scopus 로고
    • On the nature of the multivalency effect: A thermodynamic model
    • Kitov, P.I.; Bundle, D.R. On the nature of the multivalency effect: A thermodynamic model. J. Am. Chem. Soc., 2003, 125, 16271-16284.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 16271-16284
    • Kitov, P.I.1    Bundle, D.R.2
  • 13
    • 84882858329 scopus 로고    scopus 로고
    • In: Calixarenes. An Introduction; Stoddart, J. F., Ed.; The Royal Society of Chemistry: Cambridge
    • Gutsche, C.D. In: Calixarenes. An Introduction; Stoddart, J. F., Ed.; The Royal Society of Chemistry: Cambridge, 2008.
    • (2008)
    • Gutsche, C.D.1
  • 14
    • 84882920321 scopus 로고    scopus 로고
    • Calixarenes in Action Mandolini, L.; Ungaro, R. eds., Imperial College Press: London
    • Calixarenes in Action, Mandolini, L.; Ungaro, R. eds., Imperial College Press: London, 2000.
    • (2000)
  • 15
    • 84882902236 scopus 로고    scopus 로고
    • Calixarenes 2001, Z.; Böhmer, V.; Harrowfield, J.; Vicens, J. eds., Kluwer Academic Publishers: Dordrecht
    • Calixarenes 2001, Asfari, Z.; Böhmer, V.; Harrowfield, J.; Vicens, J. eds., Kluwer Academic Publishers: Dordrecht, 2001.
    • (2001)
  • 16
    • 26844450562 scopus 로고    scopus 로고
    • Calixarenes. In: Encyclopedia of Nanoscience and Nanotechnology
    • Nalwa, H. S., Ed.; American Scientific Publishers: Stevenson Ranch, 1st ed.
    • Rao, C.P.; Dey, M. Calixarenes. In: Encyclopedia of Nanoscience and Nanotechnology; Nalwa, H. S., Ed.; American Scientific Publishers: Stevenson Ranch, 2004; 1st ed., Vol. 1, pp. 475-497.
    • (2004) , vol.1 , pp. 475-497
    • Rao, C.P.1    Dey, M.2
  • 17
    • 84892021501 scopus 로고    scopus 로고
    • Calixarenes in the Nanoworld, Vicens, J.; Harrowfield, J. eds., Springer: Dordrecht
    • Calixarenes in the Nanoworld, Vicens, J.; Harrowfield, J. eds., Springer: Dordrecht, 2007.
    • (2007)
  • 18
    • 0037392207 scopus 로고    scopus 로고
    • Peptido- and glycocalixarenes: playing with hydrogen bonds around hydrophobic cavities
    • Casnati, A.; Sansone, F.; Ungaro, R. Peptido- and glycocalixarenes: playing with hydrogen bonds around hydrophobic cavities. Acc. Chem. Res., 2003, 36, 246-254.
    • (2003) Acc. Chem. Res. , vol.36 , pp. 246-254
    • Casnati, A.1    Sansone, F.2    Ungaro, R.3
  • 19
    • 77954627841 scopus 로고    scopus 로고
    • Calixarene and calixresorcarene glycosides: their synthesis and biological applications
    • Dondoni, A.; Marra, A. Calixarene and calixresorcarene glycosides: their synthesis and biological applications. Chem. Rev., 2010, 110, 4949-4977.
    • (2010) Chem. Rev. , vol.110 , pp. 4949-4977
    • Dondoni, A.1    Marra, A.2
  • 20
    • 0000128644 scopus 로고
    • p-tert-Butylcalix[4]arene [preparation]
    • Gutsche, C.D.; Iqbal, M. p-tert-Butylcalix[4]arene [preparation]. Org. Synth., 1990, 68, 234-237.
    • (1990) Org. Synth. , vol.68 , pp. 234-237
    • Gutsche, C.D.1    Iqbal, M.2
  • 21
    • 0000128641 scopus 로고
    • p-tert-Butylcalix[8]arene [preparation]
    • Munch, J. H.; Gutsche, C. D. p-tert-Butylcalix[8]arene [preparation]. Org. Synth., 1990, 68, 243-246.
    • (1990) Org. Synth. , vol.68 , pp. 243-246
    • Munch, J.H.1    Gutsche, C.D.2
  • 23
    • 0002404092 scopus 로고    scopus 로고
    • Calixarenes
    • In: Macrocyclic Synthesis: a Practical Approach; Parker, D., Ed.; Oxford University Press: Oxford
    • Arduini, A.; Casnati, A. Calixarenes. In: Macrocyclic Synthesis: a Practical Approach; Parker, D., Ed.; Oxford University Press: Oxford, 1996; pp. 145-173.
    • (1996) , pp. 145-173
    • Arduini, A.1    Casnati, A.2
  • 24
    • 0001053535 scopus 로고    scopus 로고
    • Calixarenes: from chemical curiosity to a rich source for molecular receptors
    • Casnati, A. Calixarenes: from chemical curiosity to a rich source for molecular receptors. Gazz. Chim. Ital., 1997, 127, 637-649.
    • (1997) Gazz. Chim. Ital. , vol.127 , pp. 637-649
    • Casnati, A.1
  • 25
    • 75649138627 scopus 로고    scopus 로고
    • Immobilization of calix[4]arene-based glycoclusters on TiO2 nanoparticles via click Cu(I)-catalyzed azide-alkyne coupling
    • Moni, L.; Rossetti, S.; Scoponi, M.; Marra, A.; Dondoni, A. Immobilization of calix[4]arene-based glycoclusters on TiO2 nanoparticles via click Cu(I)-catalyzed azide-alkyne coupling. Chem. Commun., 2010, 46, 475-477.
    • (2010) Chem. Commun. , vol.46 , pp. 475-477
    • Moni, L.1    Rossetti, S.2    Scoponi, M.3    Marra, A.4    Dondoni, A.5
  • 28
    • 0033572727 scopus 로고    scopus 로고
    • Interaction of sugar and anion in water via hydrogen bonding: Chain-length dependent agglutination of oligosaccharide clusters induced by multivalent anion binding
    • Hayashida, O.; Kato, M.; Akagi, K.; Aoyama, Y. Interaction of sugar and anion in water via hydrogen bonding: Chain-length dependent agglutination of oligosaccharide clusters induced by multivalent anion binding. J. Am. Chem. Soc., 1999, 121, 11597-11598.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 11597-11598
    • Hayashida, O.1    Kato, M.2    Akagi, K.3    Aoyama, Y.4
  • 29
    • 33751130579 scopus 로고
    • Sugar calixarenes: synthesis of calix[4]arenes with O-glycosyl substituents at upper and lower edges
    • Marra, A.; Scherrmann, M.C.; Dondoni, A.; Casnati, A.; Minari, P.; Ungaro, R. Sugar calixarenes: synthesis of calix[4]arenes with O-glycosyl substituents at upper and lower edges. Angew. Chem. Int. Ed., 1994, 33, 2479-2481.
    • (1994) Angew. Chem. Int. Ed. , vol.33 , pp. 2479-2481
    • Marra, A.1    Scherrmann, M.C.2    Dondoni, A.3    Casnati, A.4    Minari, P.5    Ungaro, R.6
  • 30
    • 0030831718 scopus 로고    scopus 로고
    • Synthesis and properties of O-glycosyl calix[4]arenes (calixsugars), Chem
    • Dondoni, A.; Marra, A.; Scherrmann, M.C.; Casnati, A.; Sansone, F.; Ungaro, R. Synthesis and properties of O-glycosyl calix[4]arenes (calixsugars), Chem. Eur. J. 1997, 3, 1774-1782.
    • (1997) Eur. J. , vol.3 , pp. 1774-1782
    • Dondoni, A.1    Marra, A.2    Scherrmann, M.C.3    Casnati, A.4    Sansone, F.5    Ungaro, R.6
  • 32
    • 0344820766 scopus 로고    scopus 로고
    • Amphiphilic p-tert-butylcalix[4]arene scaffolds containing exposed carbohydrate dendrons
    • Roy, R.; Kim, J.M. Amphiphilic p-tert-butylcalix[4]arene scaffolds containing exposed carbohydrate dendrons. Angew. Chem. Int. Ed., 1999, 38, 369-372.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 369-372
    • Roy, R.1    Kim, J.M.2
  • 33
    • 12344262903 scopus 로고    scopus 로고
    • Synthesis of upper rim calix[4]arene divalent glycoclusters via amide bond conjugation
    • Schädel, U.; Sansone, F.; Casnati, A.; Ungaro, R. Synthesis of upper rim calix[4]arene divalent glycoclusters via amide bond conjugation. Tetrahedron, 2005, 61, 1149-1154.
    • (2005) Tetrahedron , vol.61 , pp. 1149-1154
    • Schädel, U.1    Sansone, F.2    Casnati, A.3    Ungaro, R.4
  • 34
    • 15744377412 scopus 로고    scopus 로고
    • A synthetic divalent cholera toxin glycocalix[4]arene ligand having higher affinity than natural GM1 oligosaccharide
    • Arosio, D.; Fontanella, M.; Baldini, L.; Mauri, L.; Bernardi, A.; Casnati, A.; Sansone, F.; Ungaro, R. A synthetic divalent cholera toxin glycocalix[4]arene ligand having higher affinity than natural GM1 oligosaccharide. J. Am. Chem. Soc., 2005, 127, 3660-3661.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 3660-3661
    • Arosio, D.1    Fontanella, M.2    Baldini, L.3    Mauri, L.4    Bernardi, A.5    Casnati, A.6    Sansone, F.7    Ungaro, R.8
  • 35
    • 41149159638 scopus 로고    scopus 로고
    • Calix[4]arene decorated with four tn antigen glycomimetic units and P3CS immunoadjuvant: synthesis, characterization, and anticancer immunological evaluation
    • Geraci, C.; Consoli, G.M.L.; Galante, E.; Bousquet, E.; Pappalardo, M.; Spadaro, A. Calix[4]arene decorated with four tn antigen glycomimetic units and P3CS immunoadjuvant: synthesis, characterization, and anticancer immunological evaluation. Bioconjugate Chem., 2008, 19, 751-758.
    • (2008) Bioconjugate Chem. , vol.19 , pp. 751-758
    • Geraci, C.1    Consoli, G.M.L.2    Galante, E.3    Bousquet, E.4    Pappalardo, M.5    Spadaro, A.6
  • 37
    • 0037467380 scopus 로고    scopus 로고
    • Artificial viruses and their application to gene delivery. Size-controlled gene coating with glycocluster nanoparticles
    • Aoyama, Y.; Kanamori, T.; Nakai, T.; Sasaki, T.; Horiuchi, S.; Sando, S.; Niidome, T.; Artificial viruses and their application to gene delivery. Size-controlled gene coating with glycocluster nanoparticles. J. Am. Chem. Soc., 2003, 125, 3455-3457.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 3455-3457
    • Aoyama, Y.1    Kanamori, T.2    Nakai, T.3    Sasaki, T.4    Horiuchi, S.5    Sando, S.6    Niidome, T.7
  • 38
    • 0032715087 scopus 로고    scopus 로고
    • Synthesis of bridged thiourea calix-sugar
    • Saitz, B.C.; Torres, P.A.; Santoyo, G.F.; Synthesis of bridged thiourea calix-sugar. Synlett, 1999, 1891-1894.
    • (1999) Synlett , pp. 1891-1894
    • Saitz, B.C.1    Torres, P.A.2    Santoyo, G.F.3
  • 39
    • 0013162147 scopus 로고    scopus 로고
    • Thiourea-linked upper rim calix[4]arene neoglycoconjugates: synthesis, conformations and binding properties
    • Sansone, F.; Chierici, E.; Casnati, A.; Ungaro, R. Thiourea-linked upper rim calix[4]arene neoglycoconjugates: synthesis, conformations and binding properties. Org. Biomol. Chem., 2003, 1, 1802-1809.
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 1802-1809
    • Sansone, F.1    Chierici, E.2    Casnati, A.3    Ungaro, R.4
  • 40
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • Kolb, H.C.; Finn, M.G.; Sharpless, K.B. Click chemistry: Diverse chemical function from a few good reactions. Angew. Chem. Int. Ed., 2001, 40, 2004-2021.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 41
    • 40549092676 scopus 로고    scopus 로고
    • Conformationally mobile glucosylthioureidocalix[6]- and calix[8]arenes: Synthesis, aggregation and lectin binding
    • Sansone, F.; Baldini, L.; Casnati, A.; Ungaro, R. Conformationally mobile glucosylthioureidocalix[6]- and calix[8]arenes: Synthesis, aggregation and lectin binding. Supramol. Chem., 2008, 20, 161-168.
    • (2008) Supramol. Chem. , vol.20 , pp. 161-168
    • Sansone, F.1    Baldini, L.2    Casnati, A.3    Ungaro, R.4
  • 42
    • 48649102319 scopus 로고    scopus 로고
    • Calix[n]arene-based glycoclusters: bioactivity of thiourea-linked galactose/lactose moieties as inhibitors of binding of medically relevant lectins to a glycoprotein and cell-surface glycoconjugates and selectivity among human adhesion/growth-regulatory galectins
    • André, S.; Sansone, F.; Kaltner, H.; Casnati, A.; Kopitz, J.; Gabius, H.J.; Ungaro, R. Calix[n]arene-based glycoclusters: bioactivity of thiourea-linked galactose/lactose moieties as inhibitors of binding of medically relevant lectins to a glycoprotein and cell-surface glycoconjugates and selectivity among human adhesion/growth-regulatory galectins. ChemBioChem, 2008, 9, 1649-1661.
    • (2008) ChemBioChem , vol.9 , pp. 1649-1661
    • André, S.1    Sansone, F.2    Kaltner, H.3    Casnati, A.4    Kopitz, J.5    Gabius, H.J.6    Ungaro, R.7
  • 43
    • 0041834577 scopus 로고    scopus 로고
    • Calix[8]arene-based glycoconjugates as multivalent carbohydrate-presenting systems
    • Consoli, G.M.L.; Cunsolo, F.; Geraci, C.; Mecca, T.; Neri, P. Calix[8]arene-based glycoconjugates as multivalent carbohydrate-presenting systems. Tetrahedron Lett., 2003, 44, 7467-7470.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 7467-7470
    • Consoli, G.M.L.1    Cunsolo, F.2    Geraci, C.3    Mecca, T.4    Neri, P.5
  • 44
    • 9444263055 scopus 로고    scopus 로고
    • Synthesis and lectin binding ability of glycosamino acid-calixarenes exposing GlcNAc clusters
    • Consoli, G.M.L.; Cunsolo, F.; Geraci, C.; Sgarlata, V. Synthesis and lectin binding ability of glycosamino acid-calixarenes exposing GlcNAc clusters. Org. Lett., 2004, 6, 4163-4166.
    • (2004) Org. Lett. , vol.6 , pp. 4163-4166
    • Consoli, G.M.L.1    Cunsolo, F.2    Geraci, C.3    Sgarlata, V.4
  • 46
    • 0000299952 scopus 로고
    • Kinetics and mechanism of 1,3-dipolar cycloadditions
    • Huisgen, R. Kinetics and mechanism of 1,3-dipolar cycloadditions. Angew. Chem. Int. Ed., 1963, 2, 633-645.
    • (1963) Angew. Chem. Int. Ed. , vol.2 , pp. 633-645
    • Huisgen, R.1
  • 47
    • 0037099395 scopus 로고    scopus 로고
    • A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
    • Rostovtsev, V.V.; Green, L.G.; Fokin, V.V.; Sharpless, K.B. A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. Angew. Chem. Int. Ed., 2002, 41, 2596-2599.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 48
    • 0037012920 scopus 로고    scopus 로고
    • Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)- catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
    • Tornoe, C.W.; Christensen, C.; Meldal, M. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)- catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. J. Org. Chem., 2002, 67, 3057-3064.
    • (2002) J. Org. Chem. , vol.67 , pp. 3057-3064
    • Tornoe, C.W.1    Christensen, C.2    Meldal, M.3
  • 50
    • 33749138877 scopus 로고    scopus 로고
    • C-glycoside clustering on calix[4]arene, adamantane, and benzene scaffolds through 1,2,3-triazole linkers
    • Dondoni, A.; Marra, A. C-glycoside clustering on calix[4]arene, adamantane, and benzene scaffolds through 1,2,3-triazole linkers. J. Org. Chem., 2006, 71, 7546-7557.
    • (2006) J. Org. Chem. , vol.71 , pp. 7546-7557
    • Dondoni, A.1    Marra, A.2
  • 51
    • 34848880095 scopus 로고    scopus 로고
    • Upper rim appended hybrid calixarenes via click chemistry
    • Bew, S.P.; Brimage, R.A.; L'Hermite, N.; Sharma, S.V. Upper rim appended hybrid calixarenes via click chemistry. Org. Lett., 2007, 9, 3713-3716.
    • (2007) Org. Lett. , vol.9 , pp. 3713-3716
    • Bew, S.P.1    Brimage R.A.2    L'Hermite, N.3    Sharma, S.V.4
  • 52
    • 50149098979 scopus 로고    scopus 로고
    • Microwave-enhanced ionothermal CuAAC for the synthesis of glycoclusters on a calix[4]arene platform
    • Vecchi, A.; Melai, B.; Marra, A.; Chiappe, C.; Dondoni, A. Microwave-enhanced ionothermal CuAAC for the synthesis of glycoclusters on a calix[4]arene platform. J. Org. Chem., 2008, 73, 6437-6440.
    • (2008) J. Org. Chem. , vol.73 , pp. 6437-6440
    • Vecchi, A.1    Melai, B.2    Marra, A.3    Chiappe, C.4    Dondoni, A.5
  • 53
    • 73349131685 scopus 로고    scopus 로고
    • Achieving high affinity towards a bacterial lectin through multivalent topological isomers of calix[4]arene glycoconjugates
    • Cecioni, S.; Lalor, R.; Blanchard, B.; Praly, J.P.; Imberty, A.; Matthews, S.E.; Vidal, S. Achieving high affinity towards a bacterial lectin through multivalent topological isomers of calix[4]arene glycoconjugates. Chem. Eur. J., 2009, 15, 13232-13240.
    • (2009) Chem. Eur. J. , vol.15 , pp. 13232-13240
    • Cecioni, S.1    Lalor, R.2    Blanchard, B.3    Praly, J.P.4    Imberty, A.5    Matthews, S.E.6    Vidal, S.7
  • 55
    • 0030605882 scopus 로고    scopus 로고
    • Polysialosides scaffolded on p-tert-butylcalix[4]arene
    • Meunier, S.J.; Roy, R. Polysialosides scaffolded on p-tert-butylcalix[4]arene. Tetrahedron Lett., 1996, 37, 5469-5472.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 5469-5472
    • Meunier, S.J.1    Roy, R.2
  • 56
    • 0033597152 scopus 로고    scopus 로고
    • Preparation and host-guest interactions of novel macrocyclic sugar clusters having mono- and oligosaccharides
    • Hayashida, O.; Nishiyama, K.; Matsuda, Y.; Aoyama, Y. Preparation and host-guest interactions of novel macrocyclic sugar clusters having mono- and oligosaccharides. Tetrahedron Lett., 1999, 40, 3407-3410.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 3407-3410
    • Hayashida, O.1    Nishiyama, K.2    Matsuda, Y.3    Aoyama, Y.4
  • 57
    • 0032506686 scopus 로고    scopus 로고
    • Synthesis of carbohydrate functionalised n-propoxycalix[4]arenes
    • Felix, C.; Parrot Lopez, H.; Kalchenko, V.; Coleman, A.W. Synthesis of carbohydrate functionalised n-propoxycalix[4]arenes. Tetrahedron Lett., 1998, 39, 9171-9174.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 9171-9174
    • Felix, C.1    Parrot Lopez, H.2    Kalchenko, V.3    Coleman, A.W.4
  • 58
    • 0034751945 scopus 로고    scopus 로고
    • Synthesis of deeper calix-sugar-based on the Sonogashira reaction
    • Perez, B.F.; Santoyo, G.F. Synthesis of deeper calix-sugar-based on the Sonogashira reaction. Synlett, 2001, 1699-1702.
    • (2001) Synlett , pp. 1699-1702
    • Perez, B.F.1    Santoyo, G.F.2
  • 59
    • 33646520586 scopus 로고    scopus 로고
    • Vesicle-to-micelle transition in aqueous solutions of amphiphilic calixarene derivatives
    • Micali, N.; Villari, V.; Consoli, G.M.L.; Cunsolo, F.; Geraci, C. Vesicle-to-micelle transition in aqueous solutions of amphiphilic calixarene derivatives. Phys. Rev. E, 2006, 73, 051904-1-051904-8.
    • (2006) Phys. Rev. E , vol.73
    • Micali, N.1    Villari, V.2    Consoli, G.M.L.3    Cunsolo, F.4    Geraci, C.5
  • 60
    • 0035496031 scopus 로고    scopus 로고
    • Dependence of concanavalin A binding on anomeric configuration, linkage type, and ligand multiplicity for thiourea-bridged mannopyranosyl-beta-cyclodextrin conjugates
    • Baussanne, I.; Benito, J.M.; Mellet, C.O.; Fernandez, J.M.G.; Defaye, J. Dependence of concanavalin A binding on anomeric configuration, linkage type, and ligand multiplicity for thiourea-bridged mannopyranosyl-beta-cyclodextrin conjugates. ChemBioChem, 2001, 2, 777-783.
    • (2001) ChemBioChem , vol.2 , pp. 777-783
    • Baussanne, I.1    Benito, J.M.2    Mellet, C.O.3    Fernandez, J.M.G.4    Defaye, J.5
  • 61
    • 0036695848 scopus 로고    scopus 로고
    • Mimicking gangliosides by design: Mimics of GM1 headgroup
    • Bernardi, A.; Arosio, D.; Sonnino, S. Mimicking gangliosides by design: Mimics of GM1 headgroup. Neurochem. Res., 2002, 27, 539-545.
    • (2002) Neurochem. Res. , vol.27 , pp. 539-545
    • Bernardi, A.1    Arosio, D.2    Sonnino, S.3
  • 62
    • 0034597073 scopus 로고    scopus 로고
    • Second generation mimics of ganglioside GM1 as artificial receptors for cholera toxin: Replacement of the sialic acid moiety
    • Bernardi, A.; Carrettoni, L.; Ciponte, A.G.; Monti, D.; Sonnino, S. Second generation mimics of ganglioside GM1 as artificial receptors for cholera toxin: Replacement of the sialic acid moiety. Bioorg. Med. Chem. Lett., 2000, 10, 2197-2200.
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 2197-2200
    • Bernardi, A.1    Carrettoni, L.2    Ciponte, A.G.3    Monti, D.4    Sonnino, S.5
  • 63
    • 54349093136 scopus 로고    scopus 로고
    • Inhibition of rat glioma cell migration and proliferation by a calix[8]arene scaffold exposing multiple GlcNAc and ureido functionalities
    • Viola, S.; Consoli, G.M.L.; Merlo, S.; Drago, F.; Sortino, M.A.; Geraci, C. Inhibition of rat glioma cell migration and proliferation by a calix[8]arene scaffold exposing multiple GlcNAc and ureido functionalities. J. Neurochem., 2008, 107, 1047-1055.
    • (2008) J. Neurochem. , vol.107 , pp. 1047-1055
    • Viola, S.1    Consoli, G.M.L.2    Merlo, S.3    Drago, F.4    Sortino, M.A.5    Geraci, C.6
  • 65
    • 1242307896 scopus 로고    scopus 로고
    • From amphiphiles through nanoparticles to glycoviruses
    • Aoyama, Y. From amphiphiles through nanoparticles to glycoviruses. Chem. Eur. J., 2004, 10, 588-593.
    • (2004) Chem. Eur. J. , vol.10 , pp. 588-593
    • Aoyama, Y.1
  • 68
    • 0033236829 scopus 로고    scopus 로고
    • A macrocyclic sialic acid cluster as a host, as an adsorbate, and as a ligand for lectin and virus
    • Fujimoto, K.; Hayashida, O.; Aoyama, Y.; Guo, C.T.; Hidari, K.I.P.J.; Suzuki, Y. A macrocyclic sialic acid cluster as a host, as an adsorbate, and as a ligand for lectin and virus. Chem. Lett., 1999, 1259-1260.
    • (1999) Chem. Lett. , pp. 1259-1260
    • Fujimoto, K.1    Hayashida, O.2    Aoyama, Y.3    Guo, C.T.4    Hidari, K.I.P.J.5    Suzuki, Y.6
  • 69
    • 0001575249 scopus 로고    scopus 로고
    • Octa(galactose) derivative of calix[4]resorcarene as a versatile host in water
    • Fujimoto, T.; Shimizu, C.; Hayashida, O.; Aoyama, Y. Octa(galactose) derivative of calix[4]resorcarene as a versatile host in water. Gazz. Chim. Ital., 1997, 127, 749-752.
    • (1997) Gazz. Chim. Ital. , vol.127 , pp. 749-752
    • Fujimoto, T.1    Shimizu, C.2    Hayashida, O.3    Aoyama, Y.4
  • 70
    • 0034639983 scopus 로고    scopus 로고
    • Saccharide-directed cell recognition and molecular delivery using macrocyclic saccharide clusters: Masking of hydrophobicity to enhance the saccharide specificity
    • Fujimoto, K.; Miyata, T.; Aoyama, Y. Saccharide-directed cell recognition and molecular delivery using macrocyclic saccharide clusters: Masking of hydrophobicity to enhance the saccharide specificity. J. Am. Chem. Soc., 2000, 122, 3558-3559.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 3558-3559
    • Fujimoto, K.1    Miyata, T.2    Aoyama, Y.3
  • 72
    • 0346457142 scopus 로고    scopus 로고
    • Gene therapy needs robust synthetic nonviral platform technologies
    • Miller, A.D. Gene therapy needs robust synthetic nonviral platform technologies. ChemBioChem, 2004, 5, 53-54.
    • (2004) ChemBioChem , vol.5 , pp. 53-54
    • Miller, A.D.1


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